Abstract | BACKGROUND: OBJECTIVE: To determine the safety/tolerability and efficacy of anakinra in patients with SLE with leading joint involvement. METHODS: In patients with SLE with active polyarthritis and no other uncontrolled systemic/organ manifestations, 100 mg/day anakinra was self administered subcutaneously for 3 months. Disease activity was assessed by VAS, number of swollen/tender joints, ECLAM score, and serological and immunological measures. RESULTS: Four patients with SLE were studied; anakinra was safe in all four patients and no drug related serious adverse events occurred. A subjective benefit was seen in all patients and a trend towards better activity measures after 4 weeks. After an initial response, one patient left the study because of an arthritic flare after 6 weeks. CONCLUSION: In this study anakinra was apparently safe and well tolerated and led to clinical and serological improvement. Anakinra might be an interesting alternative in individual patients with lupus arthritis not responding to conventional treatments.
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Authors | B Ostendorf, C Iking-Konert, K Kurz, G Jung, O Sander, M Schneider |
Journal | Annals of the rheumatic diseases
(Ann Rheum Dis)
Vol. 64
Issue 4
Pg. 630-3
(Apr 2005)
ISSN: 0003-4967 [Print] England |
PMID | 15345502
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Antirheumatic Agents
- IL1RN protein, human
- Interleukin 1 Receptor Antagonist Protein
- Receptors, Interleukin-1
- Recombinant Proteins
- Sialoglycoproteins
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Topics |
- Adult
- Antirheumatic Agents
(adverse effects, therapeutic use)
- Arthritis
(drug therapy, etiology)
- Female
- Follow-Up Studies
- Humans
- Interleukin 1 Receptor Antagonist Protein
- Lupus Erythematosus, Systemic
(complications, drug therapy)
- Male
- Middle Aged
- Pain Measurement
- Pilot Projects
- Receptors, Interleukin-1
(antagonists & inhibitors)
- Recombinant Proteins
(adverse effects, therapeutic use)
- Severity of Illness Index
- Sialoglycoproteins
(adverse effects, therapeutic use)
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